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Clinical Trials/NCT02252835
NCT02252835
Completed
Phase 2

A Phase 2, Open-label, Drug-Drug Interaction Study to Evaluate the Pharmacodynamics, Pharmacokinetics, and Safety of Arhalofenate in Combination With Febuxostat for the Treatment of Hyperuricemia in Patients With Gout

CymaBay Therapeutics, Inc.1 site in 1 country32 target enrollmentAugust 2014

Overview

Phase
Phase 2
Intervention
Febuxostat
Conditions
Gout
Sponsor
CymaBay Therapeutics, Inc.
Enrollment
32
Locations
1
Primary Endpoint
Proportion of patients achieving an sUA reduction of ≥ 2.0, ≥ 3.0, and ≥ 4.0 mg/dL from baseline on Day 29 after treatment with arhalofenate 800 mg and febuxostat 80 mg
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The purpose of this study is to evaluate pharmacokinetics, pharmacodynamics, safety and potential for drug-drug interaction of arhalofenate when combined with febuxostat in adult population with gout.

Detailed Description

Patients entering the six-week Treatment Period will receive once daily oral dosing of arhalofenate during Weeks 1 and 2 (Days 1 through 14), combined once daily oral dosing of arhalofenate and febuxostat during Weeks 3 and 4 (Days 15 through 28), and once daily oral dosing of febuxostat during Weeks 5 and 6 (Days 29 through 42). In addition, all patients will receive once daily oral dosing of colchicine throughout the Treatment Period.

Registry
clinicaltrials.gov
Start Date
August 2014
End Date
December 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Male or female patient, 18 to 75 years of age, inclusive
  • Known gout diagnosis (per criteria of the American Rheumatism Association)
  • Has an sUA ≥ 7.5 mg/dL
  • A female patient must be surgically sterile or post-menopausal (at least 45 years of age with no history of menses for at least two years), or must agree to use two medically accepted methods of contraception including a barrier method for the entire duration of study participation unless she reports compete sexual abstinence. A female patient must also not be pregnant or lactating
  • Estimated creatinine clearance (eCrCl) ≥ 60 ml/min, as calculated by Cockcroft-Gault method
  • ALT or AST ≤ 3 times upper limit of normal (ULN) or total bilirubin ≤ 2 times ULN (Gilbert's syndrome is permitted)
  • All other clinical laboratory parameters must be within normal limits or considered not clinically significant
  • ECG must be normal, or if abnormal, considered not clinically significant
  • A patient who is taking a medication or agent (other than a ULT) known to influence sUA levels must be on a stable dose and regimen of the medication for at least two weeks prior to screening and must be willing to continue the same dose and regimen during study participation
  • Expected to be able to tolerate a short course of oral NSAIDs and/or oral steroids as may be needed to treat a gout flare

Exclusion Criteria

  • Treatment with any ULT (e.g., allopurinol, febuxostat, probenecid, or benzbromarone) within two weeks, or pegloticase within six months, prior to the sUA assessment at Day 1
  • Occurrence of a gout flare that has not resolved within one week prior to Day 1
  • Known or suspected secondary hyperuricemia (e.g., due to myeloproliferative disorder or organ transplant)
  • Diagnosis of xanthinuria
  • Fractional excretion of urate \> 10%
  • History of documented or suspected kidney stones within five years prior to screening
  • Known infection with the human immunodeficiency virus (HIV) or history of hepatitis B or C
  • Recent use/abuse of an illicit drug as determined by a positive urine drug screen
  • Uncontrolled hypertension that, in the opinion of the Investigator, would preclude participation in the study
  • History of stroke, transient ischemic attack, acute myocardial infarction, congestive heart failure (NYHA class II - IV), angina pectoris, coronary intervention procedure, lower extremity bypass procedure, systemic or intracoronary fibrinolytic therapy within 5 years of screening

Arms & Interventions

Arhalofenate with febuxostat (PK cohort)

Intervention: Febuxostat

Arhalofenate with febuxostat (PK cohort)

Intervention: Colchicine

Arhalofenate with febuxostat (PK cohort)

Intervention: Arhalofenate

Arhalofenate with febuxostat (non-PK cohort)

Intervention: Arhalofenate

Arhalofenate with febuxostat (non-PK cohort)

Intervention: Febuxostat

Arhalofenate with febuxostat (non-PK cohort)

Intervention: Colchicine

Outcomes

Primary Outcomes

Proportion of patients achieving an sUA reduction of ≥ 2.0, ≥ 3.0, and ≥ 4.0 mg/dL from baseline on Day 29 after treatment with arhalofenate 800 mg and febuxostat 80 mg

Time Frame: Day 29

AUC(0-tau) of arhalofenate 800 mg and febuxostat 80 mg when administered separately and in combination

Time Frame: Days 14, 28, and 42

Proportion of patients achieving a target sUA < 6.0, < 5.0, < 4.0, and < 3.0 mg/dL on Day 29 after treatment with arhalofenate 800 mg and febuxostat 80 mg

Time Frame: Day 29

Absolute and percent reduction in sUA from baseline on Day 29 after treatment with arhalofenate 800 mg and febuxostat 80 mg

Time Frame: Day 29

Tmax of arhalofenate 800 mg and febuxostat 80 mg when administered separately and in combination

Time Frame: Days 14, 28, and 42

Cmax of arhalofenate 800 mg and febuxostat 80 mg when administered separately and in combination

Time Frame: Days 14, 28, and 42

AUC(0-t) of arhalofenate 800 mg and febuxostat 80 mg when administered separately and in combination

Time Frame: Days 14, 28, and 42

Secondary Outcomes

  • Absolute and percent reduction in sUA from baseline on Day 29 after treatment with arhalofenate 600 mg and febuxostat 40 mg(Day 29)
  • Proportion of patients achieving a target sUA < 6.0, < 5.0, < 4.0, and < 3.0 mg/dL on Day 22 after treatment with arhalofenate 800 mg and febuxostat 40 mg, and with arhalofenate 600 mg and febuxostat 80 mg(Day 22)
  • Proportion of patients achieving an sUA reduction of ≥ 2.0, ≥ 3.0, and ≥ 4.0 mg/dL from baseline on Day 22 after treatment with arhalofenate 800 mg and febuxostat 40 mg, and with arhalofenate 600 mg and febuxostat 80 mg(Day 22)
  • Proportion of patients achieving an sUA reduction of ≥ 2.0, ≥ 3.0, and ≥ 4.0 mg/dL from baseline on Day 29 after treatment with arhalofenate 600 mg and febuxostat 40 mg(Day 29)
  • Proportion of patients achieving a target sUA < 6.0, < 5.0, < 4.0, and < 3.0 mg/dL on Day 29 after treatment with arhalofenate 600 mg and febuxostat 40 mg(Day 29)
  • Absolute and percent reduction in sUA from baseline on Day 22 after treatment with arhalofenate 800 mg and febuxostat 40 mg, and with arhalofenate 600 mg and febuxostat 80 mg(Day 22)
  • Proportion of patients achieving an sUA reduction of ≥ 2.0, ≥ 3.0, and ≥ 4.0 mg/dL from baseline after monotherapy treatment with arhalofenate 600 or 800 mg, or febuxostat 40 or 80 mg(Day 15 or Day 43)
  • Absolute and percent reduction in sUA from baseline on Day 15 after monotherapy treatment with arhalofenate 600 or 800 mg(Day 15)
  • Absolute and percent reduction in sUA from baseline on Day 43 after monotherapy treatment with febuxostat 40 or 80 mg(Day 43)
  • Kel and T1/2 of arhalofenate 800 mg and febuxostat 80 mg, if possible, when administered separately and in combination(Days 14, 28, and 42)
  • Proportion of patients achieving a target sUA < 6.0, < 5.0, < 4.0, and < 3.0 mg/dL after monotherapy treatment with arhalofenate 600 or 800 mg, or febuxostat 40 or 80 mg(Day 15 or Day 43)

Study Sites (1)

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